Methotrexate enhances 5-aminolevulinic acid-mediated photodynamic therapy-induced killing of human SCC4 cells by upregulation of coproporphyrinogen oxidase

摘要

Topical 5-aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) is effective for treatment of oral precancerous and cancerous lesions. This in?vitro study tried to examine whether the SCC4 cell killing by ALA-PDT was enhanced by pretreatment of methotrexate (MTX). Methods: To measure the SCC4 cell killing abilities by MTX-pretreated ALA-PDT (MTX–ALA-PDT), the SCC4 cells were pretreated with 0?mg/L, 0.001?mg/L, 0.01?mg/L, 0.1?mg/L, or 1?mg/L of MTX for 72 hours, then incubated with 0?mM, 0.0625?mM, 0.125?mM, 0.187?mM, 0.25?mM, or 0.375?mM ALA for 4 hours, and subsequently illuminated with a 640-nm light-emitting diode array at a light dose of 10?J/cm2. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was conducted at 24 hours to quantify SCC4 cell survival rates after MTX–ALA-PDT treatment. Western blot analyses were used to examine the MTX-mediated enhancement in the expressions of the heme production-related enzymes, coproporphyrinogen oxidase (CPOX), protoporphyrinogen oxidase (PPOX), and ferrochelatase, in the MTX-preconditioned SCC4 cells. Results: Pretreatment of SCC4 cells by 0.001?mg/L MTX for 72 hours resulted in a significant augmentation in MTX–ALA-PDT-induced killing of SCC4 cells (p?&?0.05). The SCC4 cells treated with 0.001?mg/L MTX for 72 hours showed a significant and 1.65-fold increase in CPOX expression compared with the control SCC4 cells without MTX treatment (p?&?0.05). However, no significant changes in the expressions of PPOX and ferrochelatase were observed in the SCC4 cells pretreated with different concentrations of MTX. Conclusion: MTX enhances ALA-PDT-induced SCC4 cell killing through upregulation of CPOX expression and subsequent increase in intracellular protoporphyrin IX production in SCC4 cells.